A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862188



Internal ID22637123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75327287..75339872hg38UCSC Ensembl
chr9:77942203..77954788hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3812586
hg1912586
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862188
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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